Hello! Describe your research question and I'll help you find matching datasets across 2,944 studies from AnVIL, BDC, CRDC, and KFDRC.

Whole Exome Sequence of 184 Individuals with 22q11.2 Deletion Syndrome

Description
Platforms
dbGaP
View in dbGaP
Summary
Consent CodesGRU-IRB
Focus / DiseasesDiGeorge Syndrome
Study DesignCase Set
Data TypesSNP/CNV Genotypes (NGS), WXS
Subjects184